Angelman Syndrome

Gene therapy could treat rare brain disorder in unborn babies

Doctors could use Crispr tool to inject benign virus into foetus’s brain to ‘switch on’ key genes.

How One Number Could Change the Lives of People With a Rare Disorder

People with Angelman syndrome now have their own unique medical code, which will make it easier to track and study the condition.

Ovid’s treatment for a rare, untreatable disease fails in a key trial

Ovid Therapeutics’ experimental drug for a devastating rare disease proved no better than placebo in a pivotal clinical trial, the company said Tuesday, a bitter disappointment for families dealing with the untreatable condition.

Diagnosing Angelman Syndrome

Many of the characteristic features of Angelman syndrome result from the loss of function of a gene called UBE3A, located on chromosome 15. UBE3A gene provides instructions for making a protein called ubiquitin protein ligase E3A. Studies suggest that ubiquitin protein ligase E3A plays a critical role in the normal development and function of the nervous system.

From UBE3A to Angelman syndrome: a substrate perspective

Angelman syndrome (AS) is a debilitating neurodevelopmental disorder that is characterized by motor dysfunction, intellectual disability, speech impairment, seizures and common features of autism spectrum disorders (ASDs).

Happy Puppet syndrome

This syndrome is characterised by bouts of laughter, intellectual retardation, cerebella ataxia and severe developmental delay, malformations of the skull and facial bones, seizures.

Life With An Angel

Disability is not an infectious disease. Disabled people are the real fighters. The only thing they are asking for, is acceptance. When you meet such a charismatic child do not avert your eyes, do not take your child away from it at school, or in the playground. Let it play with our charismatic child. Do not send it away. You can be taught a lot by a disabled child. You can learn what the real purpose in life is.

Positive Results For Ovid Drug, But Questions Remain

Even in the wildest imaginings of the company and patients, gaboxadol, also known as OV101, will not be a cure, and the data so far leave several open questions that will have to be answered by further analysis. But it may help to ease the anxiety and sleep disturbances that patients suffer throughout their lives...

The Love That Shines Through

Ten years ago, at age 3, he was given a diagnosis of Angelman syndrome, which is characterized by mental delays, jerky body motions and a good deal of smiling and laughing — Jarrett has a sweet disposition. “But then they undiagnosed him,” Mr. Rattner said. “They didn’t know what it was, but it wasn’t that.” And so the Rattners began focusing on who Jarrett was and what he could do.

What is Angelman Syndrome?

In summary, our children are missing a single gene on the approximately 20,000 genes that exist. This missing gene causes overexcitation of the brain and loss of tonic inhibition. We can either replace the missing gene or activate the silent paternal gene. It is a problem of biochemistry of the brain and not a degenerative problem. Neurons are anatomically normal, but they have poor communication (synapse). To give them back the function of UBE3A would give them a chance for a more normal life.

Angelman Foundation

Our mission is to raise money for the Angelman Respite Center. The Angelman Foundation works hand in hand with the Quebec Angelman Society to accompany families, help and support in the diagnosis of their child and guide them to the best resources.

Angelman Today

Angelman Today is made possible by article contributors from parents that share their stories and businesses that have created products and services that help support Angelman families.

Angelman Syndrome Foundation

The mission of the Angelman Syndrome Foundation is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.

Charlie Foundation

In 1993, 11 month old Charlie Abrahams developed difficult to control epilepsy. As a last resort, while Charlie was experiencing multiple daily seizures and multiple daily medications, his parents turned to a Ketogenic Diet for help. The diet worked. Charlie became seizure and drug free within a month. He was on the diet for five years and now eats whatever he wants. He has never had another seizure.

Angelman Syndrome France

Promote the expertise of parents by facilitating and organizing the dissemination of information and the pooling of their experiences.

Angelman UK

We help support people with AS and their families as well as carers of people with Angelman Syndrome. We also provide support to professionals working with the person with AS, who may have met very few or no other individuals with Angelman Syndrome in their professional career.

Global Angelman Syndrome Registry

The Global Angelman Syndrome Registry is the first online Patient Driven registry for Angelman Syndrome; putting power in the hands of those who care for someone with the Syndrome.

GARD

Angelman syndrome is a genetic disorder that primarily affects the nervous system. Characteristic features of this condition include developmental delay, intellectual disability, severe speech impairment, problems with movement and balance (ataxia), epilepsy, and a small head size.

NHS

Angelman syndrome is a genetic condition that affects the nervous system and causes severe physical and learning disabilities. A person with Angelman syndrome will have a near-normal life expectancy, but they will need support throughout their life.

NORD

Infants and children with Angelman syndrome have a distinct behavioral pattern marked by a happy demeanor with frequent and often inappropriate episodes of unprovoked, prolonged laughter and smiling.

ScienceDirect

Angelman syndrome (AS) is a neurodevelopmental disorder characterized by severe developmental delay and speech impairment, gait ataxia and/or tremulousness of limbs, microcephaly, seizures, and a unique behavior with a happy demeanor that includes frequent laughing, smiling, and excitability.